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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658504Generated: October 31, 2026

N-(2-Aminoethyl)piperidine → HCID 59987498, compound

https://huagongshe.com/reaction/658504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-Aminoethyl)piperidineHCID 33944—
ReactantHCID 59987525HCID 59987525—
ProductHCID 59987498HCID 59987498—

Reaction Steps

The title compound was prepared in the same manner described for 4-[3-({[(1-methyl-1H-indazol-5-yl)amino]carbonyl}-amino)phenoxy]-N-(2-piperidin-1-ylethyl)pyridine-2-carbox-amide, substituting 3-aminopyridine for 1-(2-aminoethyl)piperidine. 1H-NMR (DMSO-d6) δ 10.39 (s, 1H), 8.93 (s, 1H), 8.72 (s, 1H), 8.63 (d, J=5.4 Hz, 1H), 8.38 to 8.36 (m, 1H), 8.19 (d, J=8.4 Hz, 1H), 7.91 to 7.86 (m, 3H), 7.85 to 7.51 (m, 3H), 7.42 (t, J=2.1 Hz, 1H), 7.52 to 7.17 (m, 4H), 6.85 (dd, J=2.4, 1.5 Hz, 1H), 3.98 (s, 3H); MS LC-MS (M+H)+=480.1, RT=2.81 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076488B2
Source datasetuspto-grants-2011_12
ORD IDord-e8da86d447c44b07bab7715a741febd1
Source noteuspto-grants-2011_12